- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Culbertson, M. R.
- Articles by Fink, G. R.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Culbertson, M. R.
- Articles by Fink, G. R.
FRAMESHIFT SUPPRESSION IN SACCHAROMYCES CEREVISIAE. II. GENETIC PROPERTIES OF GROUP II SUPPRESSORS
Michael R. Culbertson 1, Karen M. Underbrink 2, and Gerald R. Fink 3
1 Laboratories of Genetics, University of Wisconsin, Madison, Wisconsin 53706
2 Laboratories of Molecular Biology, University of Wisconsin, Madison, Wisconsin 53706
3 Department of Biochemistry, Cornell University, Ithaca, New York 14853
Suppressors of ICR-induced mutations that exhibit behavior similar to bacterial frameshift suppressors have been identified in the yeast Saccharomyces cerevisiae. The yeast suppressors have been divided into two groups. One of these groups (Group II: SUF1, SUF3, SUF4, SUF5 and SUF6) appears to include a set of informational suppressors in which the vehicle of suppression is glycyl-tRNA. Some of the genetic properties of Group II suppressors are described in this communication.Corevertants of the Group II frameshift mutations his4519 and leu23 have been characterized to determine the spectrum of reversion events induced by the frameshift mutagen ICR-170. Seventythree ICR-induced corevertants were analyzed. With the exception of one corevertant, which carried an allele of SUF1, all carried alleles of SUF3 or SUF5. SUF1, SUF3, SUF4 and SUF6 were represented among spontaneous and UV-induced corevertants. In the course of these experiments one of the suppressors was mapped. SUF5, the probable structural gene for tRNAGLY1, is located between ade2 and ade9 on chromosome XV.SUF1, SUF4 and SUF6 have novel properties and comprise a distinct subset of suppressors. Although these suppressors show no genetic linkage to each other, they share several common features including lethality in haploid pairwise combinations, reduced tRNAGLY3 isoacceptor activity and increased efficiency of suppression in strains carrying the cytoplasmically inherited [PSI] element. In addition, strains carrying SUF1, SUF4 or SUF6 are phenotypically unstable and give rise to mitotic Suf+ segregants at high frequency. These segregants invariably contain a linked, second-site mutation that maps in or adjacent to the suppressor gene itself. Strains carrying any of these suppressors also give rise to mitotic segregants that exhibit enhanced efficiency of suppression; mutations responsible for this phenotype map at two loci, upf1 and upf2. These genes show no genetic linkage to any of the Group II suppressors.Methods that permit positive selection for mutants with decreased or enhanced efficiency of suppression have been devised in order to examine large numbers of variants. The importance of these interacting mutants is underscored by their potential utility in studying suppressor function at the molecular level.
Submitted on October 18, 1979Revised on April 15, 1980
This article has been cited by other articles:
![]() |
M. R. Culbertson Navigating Without a Road Map Genetics, September 1, 2007; 177(1): 1 - 7. [Full Text] [PDF] |
||||
![]() |
A. S. Ford, Q. Guan, E. Neeno-Eckwall, and M. R. Culbertson Ebs1p, a Negative Regulator of Gene Expression Controlled by the Upf Proteins in the Yeast Saccharomyces cerevisiae Eukaryot. Cell, February 1, 2006; 5(2): 301 - 312. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Kashima, A. Yamashita, N. Izumi, N. Kataoka, R. Morishita, S. Hoshino, M. Ohno, G. Dreyfuss, and S. Ohno Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay Genes & Dev., February 1, 2006; 20(3): 355 - 367. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. HARGER and J. D. DINMAN Evidence against a direct role for the Upf proteins in frameshifting or nonsense codon readthrough RNA, November 18, 2004; 10(11): 1721 - 1729. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Shirley, A. S. Ford, M. R. Richards, M. Albertini, and M. R. Culbertson Nuclear Import of Upf3p Is Mediated by Importin-{alpha}/-{beta} and Export to the Cytoplasm Is Required for a Functional Nonsense-Mediated mRNA Decay Pathway in Yeast Genetics, August 1, 2002; 161(4): 1465 - 1482. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. T. Bond, D. A. Mangus, F. He, and A. Jacobson Absence of Dbp2p Alters Both Nonsense-Mediated mRNA Decay and rRNA Processing Mol. Cell. Biol., November 1, 2001; 21(21): 7366 - 7379. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. He and A. Jacobson Upf1p, Nmd2p, and Upf3p Regulate the Decapping and Exonucleolytic Degradation of both Nonsense-Containing mRNAs and Wild-Type mRNAs Mol. Cell. Biol., March 1, 2001; 21(5): 1515 - 1530. [Abstract] [Full Text] |
||||
![]() |
J. L. Hendrick, P. G. Wilson, I. I. Edelman, M. G. Sandbaken, D. Ursic, and M. R. Culbertson Yeast Frameshift Suppressor Mutations in the Genes Coding for Transcription Factor Mbf1p and Ribosomal Protein S3: Evidence for Autoregulation of S3 Synthesis Genetics, March 1, 2001; 157(3): 1141 - 1158. [Abstract] [Full Text] |
||||
![]() |
A. B. Maderazo, F. He, D. A. Mangus, and A. Jacobson Upf1p Control of Nonsense mRNA Translation Is Regulated by Nmd2p and Upf3p Mol. Cell. Biol., July 1, 2000; 20(13): 4591 - 4603. [Abstract] [Full Text] |
||||
![]() |
J. H.-N. Ho and A. W. Johnson NMD3 Encodes an Essential Cytoplasmic Protein Required for Stable 60S Ribosomal Subunits in Saccharomyces cerevisiae Mol. Cell. Biol., March 1, 1999; 19(3): 2389 - 2399. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. G. McCarthy Posttranscriptional Control of Gene Expression in Yeast Microbiol. Mol. Biol. Rev., December 1, 1998; 62(4): 1492 - 1553. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Lew, S. Enomoto, and J. Berman Telomere Length Regulation and Telomeric Chromatin Require the Nonsense-Mediated mRNA Decay Pathway Mol. Cell. Biol., October 1, 1998; 18(10): 6121 - 6130. [Abstract] [Full Text] |
||||
![]() |
R. Shirley, M. Lelivelt, L. Schenkman, J. Dahlseid, and M. Culbertson A factor required for nonsense-mediated mRNA decay in yeast is exported from the nucleus to the cytoplasm by a nuclear export signal sequence J. Cell Sci., January 11, 1998; 111(21): 3129 - 3143. [Abstract] [PDF] |
||||
![]() |
Y Cui, K W Hagan, S Zhang, and S W Peltz Identification and characterization of genes that are required for the accelerated degradation of mRNAs containing a premature translational termination codon. Genes & Dev., February 15, 1995; 9(4): 423 - 436. [Abstract] [PDF] |
||||
![]() |
F He and A Jacobson Identification of a novel component of the nonsense-mediated mRNA decay pathway by use of an interacting protein screen. Genes & Dev., February 15, 1995; 9(4): 437 - 454. [Abstract] [PDF] |
||||
![]() |
P Leeds, S W Peltz, A Jacobson, and M R Culbertson The product of the yeast UPF1 gene is required for rapid turnover of mRNAs containing a premature translational termination codon. Genes & Dev., December 1, 1991; 5(12a): 2303 - 2314. [Abstract] [PDF] |
||||
![]() |
T. Donahue, P. Farabaugh, and G. Fink Suppressible four-base glycine and proline codons in yeast Science, April 24, 1981; 212(4493): 455 - 457. [Abstract] [PDF] |
||||







